Effect of Sea Grapes-antioxidants Extract in Obese Men : 4 Weeks Randomized-Double Blind Controlled Trial
Effect of Sea Grapes-antioxidants Extract in Obese Men
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
The study was a 4-week, randomized, double-blind, placebo-controlled clinical trial followed by a 1-week screening period. Participants who respond to the invitation and meet the entry criteria during the telephone screening interview are scheduled for the initial visit. Evaluation during the initial visit includes physical examination in the form of BMI (Body Mass Index) based on Asia-Pacific guidelines and blood parameter screening tests in the form of blood glucose, triglycerides, high-density lipoprotein (HDL), low-density lipoprotein (LDL) and total cholesterol, and PGC-1α were performed on all participants within 1 week of the initial screening. A random number between 1 and 70 was generated for each subject and registered participants were scheduled for their first visit and randomly assigned to the sea grape extract group (n=35) or placebo (n=35). Sea grape extract/placebo tablets/capsules were given to participants every 1 week (1 day of consumption per oral) 15 Minutes before eating (According to the diabetes drug guidline consumtion).
During the 4-week intervention period, participants were asked to continue their usual diet and not to consume functional foods or other dietary supplements. Anthropometry (BMI), Waist Hip Ratio (WHR) , blood parameters, urine profile (Marker of toxicity), and nutrient intake of both groups were measured before and after the intervention period. During the trial phase, all participants were instructed to maintain their normal diet and physical activity. Each week participants were asked to report assessments of side effects or changes in training, lifestyle, or diet; and to evaluate tablet compliance.
Subjects/Participants The study participants were recruited during 2021 at Manado, Republic of Indonesia. A total of 150 participants agreed to participate in the study. Only individuals men who are obese (BMI ≥ 25 kg m-2 and Waist Hip Ratio (WHR) ≥ 0.90) according to Asia-Pacific guidelines and have not been diagnosed with other diseases were included in the study. To meet guidelines for evaluating the efficacy of functional food referring to the Korea Food and Drug Administration (because Indonesia does not yet exist and Koreas belong to one Asian region so used), very obese participants (BMI ≥ 30 kg m-2) were not included in the study.
In total, 70 participants met the research criteria (age 29.98 ± 3.26 year; weight, ..... ± .... kg; BMI, .... ±.... kg m-2) and were randomly divided into two groups (n = 35 each) given sea grape extract 1.68 g/70kg BB day-1) or placebo (1.68 g/70kg BB day-1). The exclusion criteria for this study are as follows: (a) significant weight variation (over 10%) in the last 3 months; (b) a history of cardiovascular disease including arrhythmia, heart failure, or myocardial infarction, diabetes mellitus (DM) and the use of pacemakers; (c) a history of conditions that may interfere with test products or inhibit their absorption such as gastrointestinal diseases (Crohn's disease) or surgeries that have been experienced (caesarean section or enterocele); (d) participation in other clinical trials in the last 2 months; (e) abnormal liver function; (f) a history of kidney disease (eg, acute or chronic renal failure and nephrtic syndrome); (g) undergo antipsychotic drug therapy within the last 2 months; (h) laboratory test results as well as medical or psychological conditions that may interfere with successful participation in research assessed by researchers; (i) a history of alcohol or substance abuse; and (j) allergy or hypersensitivity to any of the ingredients in the test product; (k) is neither a passive nor an active smoker. All participants give written consent before the investigation begins. The research protocol was submitted to the Health Research Ethics Commission (KEPK) of The General Hospital of Education Prof. Dr. RD. Kandou (Manado, Republic of Indonesia) online at http://sim-epk.keppkn.kemkes.go.id. All protocols referred to The Declaration of Helsinki and The Council for International Organizations of Medical Sciences (CIOMS).
Measurement of Efficacy Results A total of 70 participants who met the research criteria were asked to visit the clinic once every 1 week (0th, 1st, 2nd, 3rd, and 4th/last week of the study period) with a total of 5 clinical visits including initial examination. During each visit, the use of the supplement is currently reviewed and symptoms or side effects are noted. During screening visits, demographic and lifestyle information is collected (age, alcohol consumption, and smoking habits). Medical history is taken and urine turbidity tests are carried out.
The following parameters are assessed; Weight, Height, WHR and BMI during each visit. Blood samples were collected after a minimum of 12 hours of fasting during initial screening as well as in the 0, 2nd and 4th weeks of the intervention period to obtain blood glucose profiles, total cholesterol, triglycerides, high-density lipoprotein (HDL), low-density lipoprotein (LDL) and PGC-1α. Blood samples were taken from the arm vein. The arm vein to be punctured is cleaned with 70% alcohol and allowed to dry. A tourniquet is placed on the upper arm to expose and slightly accentuate the veins. The skin is stretched over the vein with the fingers of the left hand so that the vein cannot move. The skin is pierced with a needle and syringe with the right hand until the tip of the needle enters the lumen of the vein. The tourniquet is removed and slowly withdraw the syringe suction until the desired amount of blood is obtained. A 70% alcohol swab is placed over the needle and the syringe and needle are removed. The needle is removed from the syringe and the blood sample is transferred into a vacutainer tube.
Evaluation of Safety and Diet
The safety of the extract is assessed by the following procedure. Urine Test Strips 10 Verify Parameters, Parameters examined are:
- Glucose (50 -100 mg / dl)
- Protein (7.5 - 15 mg / dl)
- pH (5-9)
- Leukocytes (9-15 leu / ul)
- Nitrite (0.05-0.1 mg/ dl)
- Urobilinogen (0.2-1.0 mg / dl)
- Blood (5-10 Ery/ul)
- Ketones (2.5-5 mg/dl)
- Bilirubin (0.4-1.0 mg/ dl)
- Specific Gravity (SG) (1,000-1,030) Test the urine parameters above using Urinalysis 10U Reagent Strips Verify (REF U031-102 exp. 2022-03-05). Pulse rate and blood pressure are measured on each visit after a 5-minute break using intelliVue MP70 (Philips, Netherlands). Personal reports are also recorded at these times. We kept the subjects maintaining their usual diet and activity, and all participants completed diet records on each visit to the clinic during the intervention period to evaluate their energy intake and diet quality. Food intake data were analyzed by a nutritionist (Melvin Junior Tanner, S.Gz).
Statistical Analysis Statistical analysis is performed using SPSS software, version 26 (IBM Corporation). Fixed effects include treatment groups, treatment visits, and interactions between treatment and visit groups. The value p<0.05 is considered statistically significant.
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Early Phase 1
Contacts and Locations
Study Locations
-
-
Sulawesi Utara
-
Manado, Sulawesi Utara, Indonesia, 95115
- Fahrul Nurkolis
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Only individuals men who are obese (BMI ≥ 25 kg m-2) according to Asia-Pacific guidelines
- Waist Hip Ratio (WHR) ≥ 0.90 according to Asia-Pacific guidelines and
- not been diagnosed with other diseases were included in the study.
Exclusion Criteria:
- (a) significant weight variation (over 10%) in the last 3 months;
- (b) a history of cardiovascular disease including arrhythmia, heart failure, or myocardial infarction, diabetes mellitus (DM) and the use of pacemakers;
- (c) a history of conditions that may interfere with test products or inhibit their absorption such as gastrointestinal diseases (Crohn's disease) or surgeries that have been experienced (caesarean section or enterocele);
- (d) participation in other clinical trials in the last 2 months;
- (e) abnormal liver function;
- (f) a history of kidney disease (eg, acute or chronic renal failure and nephrtic syndrome);
- (g) undergo antipsychotic drug therapy within the last 2 months;
- (h) laboratory test results as well as medical or psychological conditions that may interfere with successful participation in research assessed by researchers;
- (i) a history of alcohol or substance abuse; and
- (j) allergy or hypersensitivity to any of the ingredients in the test product;
- (k) is neither a passive nor an active smoker.
- All participants give written consent before the investigation begins.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Placebo Comparator: placebo A
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo B
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo C
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo D
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo E
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo F
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo G
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo H
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo I
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo J
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo K
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo L
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo M
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo N
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo O
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo P
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo Q
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo R
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo S
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Placebo Comparator: placebo T
placebo lactose powder (1.68 g/70kg BW day-1) or placebo tablets were given to this group/arms
|
placebo lactose powder (1.68 g/70kg BW day-1).
|
|
Experimental: sea grape extract A
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract B
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract C
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract D
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract E
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract F
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract G
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract H
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract I
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract J
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract K
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract L
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract M
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract N
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract O
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract P
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract Q
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract R
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract S
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
|
Experimental: sea grape extract T
given sea grape extract 1.68 g/70kg BB day-1 were given to this group/arms
|
Contains antioxidants 45.66 ± 0.55% and Caulerpin.
Sea grapes are usually consumed raw without any indication of poisoning.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Peroxisome proliferator-activated receptor (PPAR)-γ coactivator 1 alpha (PGC-1α) Levels "change" is being assessed
Time Frame: Change from Baseline PGC-1α Levels at 4th weeks of the intervention period
|
Evaluate PGC-1α level in pg/dL
|
Change from Baseline PGC-1α Levels at 4th weeks of the intervention period
|
|
Total Cholesterol "change" is being assessed
Time Frame: Change from Baseline Total Cholesterol at 4th weeks of the intervention period
|
Evaluate total Cholesterol level in mg/dL
|
Change from Baseline Total Cholesterol at 4th weeks of the intervention period
|
|
Blood Glucose "change" is being assessed
Time Frame: Change from Baseline Blood Glucose at 4th weeks of the intervention period
|
Evaluate total blood sugar level in mg/dL
|
Change from Baseline Blood Glucose at 4th weeks of the intervention period
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body Mass Index (BMI)
Time Frame: Change from Baseline Body Mass Index (BMI) at 4th weeks of the intervention period
|
Body Mass Index (BMI) weight and height will be combined to report BMI in kg/m^2
|
Change from Baseline Body Mass Index (BMI) at 4th weeks of the intervention period
|
|
Triglycerides
Time Frame: Change from Baseline Triglycerides Levels at 4th weeks of the intervention period
|
Triglycerides in mg/dL
|
Change from Baseline Triglycerides Levels at 4th weeks of the intervention period
|
|
high-density lipoprotein (HDL)
Time Frame: Change from Baseline high-density lipoprotein (HDL) Levels at 4th weeks of the intervention period
|
high-density lipoprotein (HDL) in mg/dL
|
Change from Baseline high-density lipoprotein (HDL) Levels at 4th weeks of the intervention period
|
|
low-density lipoprotein (LDL)
Time Frame: Change from Baseline low-density lipoprotein (LDL) Levels at 4th weeks of the intervention period
|
low-density lipoprotein (LDL) in mg/dL
|
Change from Baseline low-density lipoprotein (LDL) Levels at 4th weeks of the intervention period
|
|
Body Weight
Time Frame: Change from Baseline Body Weight at 4th weeks of the intervention period
|
Weight in kilograms (kg)
|
Change from Baseline Body Weight at 4th weeks of the intervention period
|
|
Body Height
Time Frame: Change from Baseline Body Height at 4th weeks of the intervention period
|
Height in meters (M)
|
Change from Baseline Body Height at 4th weeks of the intervention period
|
|
waist-to-hip ratio (WHR)
Time Frame: Change from Baseline waist-to-hip ratio (WHR) at 4th weeks of the intervention period
|
This is calculated as waist measurement divided by hip measurement (W⁄H).
For example, a person with a 30" (76 cm) waist and 38" (97 cm) hips has a waist-hip ratio of about 0.78.
|
Change from Baseline waist-to-hip ratio (WHR) at 4th weeks of the intervention period
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Fahrul Nurkolis, UIN Sunan Kalijaga Yogyakarta
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- 7171011P321452021061500018
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- Statistical Analysis Plan (SAP)
- Clinical Study Report (CSR)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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